Emiy Yokoyama
Mexico, MEX, Mexico
Last Updated: 09/26/2026
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Found 10 publications
A progeria syndrome links DNA hypermethylation to age-related pathology.
Journal: Nature genetics
Published: April 07, 2025
Inherited bone marrow failure syndromes: phenotype as a tool for early diagnostic suspicion at a major reference center in Mexico.
Journal: Frontiers in genetics
Published: September 13, 2023
Dysgerminoma Probably Due to a Novel SOHLH1-pathogenic Variant Causing Familial Ovarian Dysgenesis.
Journal: Reproductive sciences (Thousand Oaks, Calif.)
Published: May 05, 2023
Frequent copy number variants in a cohort of Mexican-Mestizo individuals.
Journal: Molecular cytogenetics
Published: November 01, 2022
Non-classical 1p36 deletion in a patient with Duane retraction syndrome: case report and literature review.
Journal: Molecular cytogenetics
Published: May 30, 2020
7p15 deletion as the cause of hand-foot-genital syndrome: a case report, literature review and proposal of a minimum region for this phenotype.
Journal: Molecular cytogenetics
Published: September 04, 2017
Influence of SNPs in Genes that Modulate Lung Disease Severity in a Group of Mexican Patients with Cystic Fibrosis.
Journal: Archives of medical research
Published: February 04, 2016
Interstitial deletion of 2q24.2: further delineation of an emerging syndrome associated with intellectual disability, severe hypotonia and moderate intrauterine growth restriction.
Journal: American journal of medical genetics. Part A
Published: April 23, 2013
Genotype-phenotype correlation in a sample of Mexican patients with cystic fibrosis
Journal: Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion
Published: February 06, 2013
Showing 1-10 of 10
Last Updated: 09/26/2026